Allele Registry

Canonical Allele Identifier: PA112925

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015493

RCV000712217

ClinVar Variation:

14412

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Asp564Gly	CA123935 NM_000233.4:c.1691A>G